MEMO 4D Curve™ Semirigid mitral annuloplasty ring

by Corcym S.r.l. 510(k)

Active United States

510(k) K261707

Regulatory status

as of 26 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESE Substantially Equivalent · Special	NumberK261707	Date18 Jun 2026Cleared	StatusActive

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not known
Not covered

United States — FDA 510(k) Active

Recalls: none on record (FDA, checked 25 Oct 2026)

Specification

510(k)

510(k) Number: K261707
FDA Product Code: KRH

Device Class: Class II
Regulation: 21 CFR Part 870.3800
Advisory Committee: Cardiovascular
FDA Decision: SESE Substantially Equivalent

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